Methanesulfonate → HCID 488380, 화합물

반응식

[C:1]1([CH:7]2[NH:12][CH2:11][CH2:10][N:9]([C:13]3[N:22]=[C:21]4[C:16]([C:17](=[O:30])[C:18]([C:27]([OH:29])=[O:28])=[CH:19][N:20]4[C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:15][C:14]=3[F:31])[CH2:8]2)C=CC=CC=1.[CH3:32]S([O-])(=O)=O>>[CH3:1][CH:7]1[N:12]([CH3:32])[CH2:11][CH2:10][N:9]([C:13]2[N:22]=[C:21]3[C:16]([C:17](=[O:30])[C:18]([C:27]([OH:29])=[O:28])=[CH:19][N:20]3[C:23]([CH3:24])([CH3:25])[CH3:26])=[CH:15][C:14]=2[F:31])[CH2:8]1

참가 물질

반응물 2

HCID 85257Methanesulfonate

HCID 488306HCID 488306, 화합물

생성물 1

HCID 488380HCID 488380, 화합물

실험 절차

7-(3-phenyl-1-piperazinyl)-1-(1,1-dimethylethyl)-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid, methanesulfonate.

출처 및 근거

ORD 기록: ord-be0cc4cab6c748eaa686b88408075d6b
출처 데이터셋: uspto-grants-1990_09
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US04954507

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